Effect of capacitive coupled electrical stimulation on regenerate bone

• Published in: Journal of orthopaedic research Vol. 14; no. 2; p. 296
• Main Authors: Pepper, J R, Herbert, M A, Anderson, J R, Bobechko, W P
• Format: Journal Article
• Language: English
• Published: United States 01-03-1996
• Subjects: Animals; Biomechanical Phenomena; Bone and Bones - anatomy & histology; Bone and Bones - diagnostic imaging; Bone and Bones - physiology; Bone Regeneration - physiology; Dogs; Electric Conductivity; Electric Stimulation Therapy - methods; Fracture Healing; Ilizarov Technique; Male; Osteogenesis - physiology; Radiography; Treatment Outcome
• ISSN: 0736-0266
• DOI: 10.1002/jor.1100140219

An in vivo study was carried out to determine if capacitive coupled electrical stimulation increased the rate of recovery of strength of regenerate bone produced as a result of lengthening by the Ilizarov technique. Thirty-four adult male beagles underwent a right tibial mid-diaphyseal corticotomy, followed by a 5-day delay, and then 21 days of lengthening (1 mm/day). At the start of the post-distraction period (day 27), stimulation (3-6.3 V peak to peak, 5-10 mA root-mean-square at 60 kHz) was applied for 28 days to one group. The nonstimulated group (n = 17) underwent a 28-day period with no stimulation. From each group, four tibiae were prepared for histology; both ends of the remaining bones were embedded in polymethylmethacrylate and tested in torsion (internal rotation at 4.7 degrees/sec) until failure. Statistically significant changes included a 37% lower maximum torque capacity and a 40% decrease in strain energy to failure in the stimulated group compared with the nonstimulated group. The findings are supported by measured trends to a lower modulus of rigidity (37% decrease) and a smaller percentage of active osteoid perimeter (20% decrease) for the stimulated group. The experimental data suggest that when this dose of capacitive coupled electrical stimulation is applied to the regenerating bone created during distraction osteogenesis, it delays the recovery of bone strength compared with an untreated control.